Midodrine Hydrochloride
- Product NDC
- 72162-1517
- 11-digit product format
- 721621517
- Labeler code
- 72162
- Product ID
- 72162-1517_c4296ad6-f454-4e6e-bf0b-2c1fc5d7271e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207169
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Midodrine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MIDODRINE HYDROCHLORIDE | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 59JV96YTXV |
| Rxcui | 993466 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1517-1 | Midodrine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1517 | MIDODRINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20231007_17b24a0b-03e4-4b58-87ab-3d66fec30226.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1517-1 | 72162151701 | 100 TABLET in 1 BOTTLE (72162-1517-1) | 100 tablet | 2023-10-06 | No | No | Current |